DSpace at RU >

Browsing by Author Poirier, K.

Full Text	Issue Date	Title	Author(s)
	2011	Mutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disability	Pagan, C.; Botros, H.G.; Poirier, K.; Dumaine, A.; Jamain, S., et al
	2007	Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium.	Brouwer, A.P.M. de; Yntema, H.G.; Kleefstra, T.; Lugtenberg, D.; Oudakker, A.R., et al
	2006	Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis.	Poirier, K.; Lacombe, D.; Gilbert-Dussardier, B.; Raynaud, M.; Desportes, V., et al
	2005	Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males.	Poirier, K.; Francis, F.; Hamel, B.C.J.; Moraine, C.; Fryns, J.P., et al